Evaluation of Efficacy and Safety of Clevira as an Add on Drug in Mild to Moderate COVID-19 Positive Patients- A Randomised Control Trial
Journal of Clinical and Diagnostic Research
; 16(2):KC01-KC07, 2022.
Article
in English
| EMBASE | ID: covidwho-1677771
ABSTRACT
Introduction:
Coronavirus Disease 2019 (COVID-19) has caused a devastating pandemic. Despite the worldwide efforts to find a therapeutic strategy and prophylaxis, we have not attained a complete success. Hence, there exists an urgent need for development of alternative solutions from Ayurveda system of medicine for COVID-19.Aim:
To evaluate clevira, a polyherbal ayurvedic formulation, for its efficacy and safety in treatment of mild to moderate COVID-19 patients as an add on drug. Materials andMethods:
This randomised control trial was carried out from May 2020 to July 2020, in 100 patients (50 in test group and 50 in control group) confirmed with COVID-19 infection (mild to moderate cases) by Reverse Transcription Polymerase Chain Reaction (RT-PCR) at a tertiary care Government Medical College and Hospital in Chennai, India. The test group received tablet clevira orally twice daily after food, in the morning and night for 14 days, as an add on, in addition to standard care of treatment as received by the control group. The primary outcome was assessment of clinical recovery, proportion of patients with swabs negative for COVID-19 in RT-PCR and reduction of Viral cycle threshold ratio. The results of the both group were analysed and compared using Chi-square test and student's t-test.Results:
Significant improvement (p-value=0.0338) was seen in patients on day 5, who got treated with clevira as add on drug. An 86% (43) of patients turned out to be COVID-19 RT-PCR test negative on day 5 while in the control group 66% (33) of patients turned out to be negative. There was a statistically significant difference (p-value=0.0196) between the test and control groups on comparing the mean difference in CT value results between day 1 and day 5. Clevira when given in addition to the standard of care, showed a significant improvement in signs and symptoms of COVID-19 infection.Conclusion:
Clevira, with its polyherbal ingredients show a significant antiviral action against coronavirus when given in addition to the standard of care medications suggested by Indian Council of Medical Research (ICMR), over a period of 14 days in treatment of mild to moderate COVID-19 patients.
adult; Andrographis paniculata; antiviral activity; article; Ayurveda; black pepper; comparative effectiveness; controlled study; coronavirus disease 2019; drug safety; female; government; health care quality; human; India; major clinical study; male; medical research; medical school; night; nonhuman; outcome assessment; prophylaxis; randomized controlled trial; reverse transcription polymerase chain reaction; systems medicine; tertiary health care; Tinospora cordifolia; antivirus agent
Full text:
Available
Collection:
Databases of international organizations
Database:
EMBASE
Type of study:
Experimental Studies
/
Randomized controlled trials
Language:
English
Journal:
Journal of Clinical and Diagnostic Research
Year:
2022
Document Type:
Article
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